A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15220385



Internal ID6836550
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38007936..38032983hg38UCSC Ensembl
Innerchr15:38007997..38032922hg38UCSC Ensembl
Outerchr15:38007875..38033044hg38UCSC Ensembl
chr15:38300137..38325184hg19UCSC Ensembl
Innerchr15:38300198..38325123hg19UCSC Ensembl
Outerchr15:38300076..38325245hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3825048
hg1925048
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636185
Supporting Variants
SamplesNA20905
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15220385
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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